Ruba Kado1, Georgiana Sanders, W Joseph McCune. 1. aDivision of Rheumatology, Department of Internal Medicine bDivision of Allergy and Immunology, Departments of Internal Medicine and Pediatrics and Communicable Diseases, University of Michigan, Michigan, USA.
Abstract
PURPOSE OF REVIEW: There are no established guidelines for evaluating and treating hypogammaglobulinemia in patients with rheumatic disease who receive B-cell depleting agents. The purpose of this article is to review findings in the work-up and treatment of common variable immunodeficiency (CVID) that can guide our evaluation of patients with autoimmune disease who develop hypogammaglobulinemia after rituximab/B-cell depleting therapy. RECENT FINDINGS: Infection rates are higher in rheumatic disease patients who develop hypogammaglobulinemia than those who do not. However, not all patients who develop hypogammaglobulinemia are at increased risk of developing infection after B-cell depleting therapy. Recent consensus statements have helped refine the diagnosis of impaired immune responses in patients with CVID, and can provide guidance for the diagnostic work-up and therapeutic decision making for patients with secondary drug induced hypogammaglobulinemia. SUMMARY: Based on findings in studies of CVID, assessment of vaccine response in patients with hypogammglogulinemia after rituximab therapy in the setting of recurrent infections can help predict propensity for infection and thus guide decision making with regards to intravenous immunoglobulin supplementation and retreatment with rituximab.
PURPOSE OF REVIEW: There are no established guidelines for evaluating and treating hypogammaglobulinemia in patients with rheumatic disease who receive B-cell depleting agents. The purpose of this article is to review findings in the work-up and treatment of common variable immunodeficiency (CVID) that can guide our evaluation of patients with autoimmune disease who develop hypogammaglobulinemia after rituximab/B-cell depleting therapy. RECENT FINDINGS:Infection rates are higher in rheumatic diseasepatients who develop hypogammaglobulinemia than those who do not. However, not all patients who develop hypogammaglobulinemia are at increased risk of developing infection after B-cell depleting therapy. Recent consensus statements have helped refine the diagnosis of impaired immune responses in patients with CVID, and can provide guidance for the diagnostic work-up and therapeutic decision making for patients with secondary drug induced hypogammaglobulinemia. SUMMARY: Based on findings in studies of CVID, assessment of vaccine response in patients with hypogammglogulinemia after rituximab therapy in the setting of recurrent infections can help predict propensity for infection and thus guide decision making with regards to intravenous immunoglobulin supplementation and retreatment with rituximab.
Authors: Paul Brogan; Rae S M Yeung; Gavin Cleary; Satyapal Rangaraj; Ozgur Kasapcopur; Aimee O Hersh; Suzanne Li; Dusan Paripovic; Kenneth Schikler; Andrew Zeft; Claudia Bracaglia; Despina Eleftheriou; Pooneh Pordeli; Simone Melega; Candice Jamois; Jacques Gaudreault; Margaret Michalska; Paul Brunetta; Jennifer C Cooper; Patricia B Lehane Journal: Arthritis Rheumatol Date: 2021-12-05 Impact factor: 15.483